Medicament device for use with a conventional syringe

ABSTRACT

The novel medicament devices comprise a housing that preferably contains a preloaded, conventional syringe with medication. Both trained and untrained users may administer an injection safely and conveniently to themselves or others in myriad settings. Certain of the disclosed embodiments rely on the user&#39;s manual action to insert the needle. Only after the needle is fully inserted is the medicament delivered, resulting in a safer injection. After use, the devices include a locking mechanism that locks a spring-loaded sheath in place around the needle for protection. As a common syringe is utilized, engineering and production issues of conventional automatic injectors are avoided.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application claims benefit of and priority to U.S. patent application Ser. No. 15/707,111 filed on Sep. 18, 2017, and U.S. Provisional Patent Application Ser. No. 62/507,077 filed on May 16, 2017. Each application is incorporated by reference as if fully set forth herein.

BACKGROUND

The present disclosure relates generally to a device for injecting or otherwise administrating a medication.

SUMMARY

One exemplary embodiment of the disclosed subject matter is a hand-held device comprising a body assembly preferably configured to receive a conventional syringe. The body assembly has a top and an opposing bottom. A housing cap is disposed at the top of the body assembly. A first spring is disposed between the body assembly and housing cap. The body assembly may comprise a housing, a sheath slideably contained within the housing, a sheath lock disposed within the housing opposite the sheath, and a second spring disposed within the sheath lock.

The medicament device may further comprise a sheath clip disposed in an annular groove within the housing for retaining the sheath during handling of the device. The device may also include a sheath cap disposed about the bottom of the body assembly. The sheath lock is preferably configured to frictionally engage flanges of a barrel of a conventional syringe. The housing and sheath are each preferably substantially the same length as the syringe barrel. The second spring preferably requires less compression force than the first spring.

Another exemplary embodiment of the disclosed subject matter is a device for administering medicament using a conventional syringe, wherein the device comprises a body assembly configured to receive the syringe. The body assembly has a top and an opposing bottom. A housing cap is disposed at the top of the body assembly. The body assembly preferably comprises a housing, a sheath slideably contained within the housing, a locking mechanism, and a sheath spring.

The locking mechanism may comprise a sleeve, sleeve tracks, and one or more sheath pins, wherein the sleeve is slideably disposed within the housing at an end opposite the sheath, wherein the sheath pins protrude from the interior of the sheath, and wherein the sleeve tracks are cut within the sleeve and configured to engage the one or more sheath pins. The sleeve tracks may be bifurcated to lock the sheath in place around a needle of the syringe after use of the device to administer medicament. The locking mechanism may further comprise sheath snaps extending from the interior of the sheath, wherein the sheath snaps may be engaged by sheath fingers extending from one end of the sheath.

In the alternative, the locking mechanism may comprise a sheath lock disposed within the housing at an end opposite the sheath. The sheath lock is preferably configured to frictionally engage flanges of the syringe barrel. The device of this arrangement may further comprise a plunger spring disposed between the housing cap and the housing, wherein the plunger spring requires more compression force than the sheath spring.

Yet another exemplary embodiment of the disclosed subject matter is a method of using a device for administering medicament using a conventional syringe having a needle. The method may comprise utilizing a primary stroke to slide a sheath into a housing body containing the syringe and thereby expose the needle, wherein the primary stroke must overcome the force of a sheath spring biasing the sheath away from the housing body. The method may further comprise utilizing a secondary stroke to administer medicament contained within the syringe after the primary stroke is complete. After the secondary stroke is complete, a locking mechanism of the device may preclude the use of another primary stroke.

Another exemplary embodiment of the disclosed subject matter is a device for administering medicament using a conventional syringe, wherein the device comprises a body assembly configured to receive the syringe. A top assembly is disposed at the top of the body assembly, wherein the body assembly comprises a sheath, a sheath spring, and a sleeve. The top assembly comprises a top, a pusher spring, and a pusher. The sheath may have one or more sheath pins, and the sleeve may have tracks configured to receive the one or more sheath pins. The body assembly may further comprise a body configured to receive the sheath, sheath spring, and sleeve. The medicament device may further comprise a cap assembly at the bottom of the body. In the alternative, the medicament device may further comprise a cap assembly at the bottom of the top. The sheath is preferably substantially the same length as a barrel of a conventional syringe. Moreover, the sheath spring preferably requires less compression force than the pusher spring.

BRIEF DESCRIPTION OF THE DRAWINGS

Some non-limiting exemplary embodiments of the disclosed subject matter are illustrated in the following drawings. Identical or duplicate or equivalent or similar structures, elements, or parts that appear in one or more drawings are generally labeled with the same reference numeral, optionally with an additional letter or letters to distinguish between similar objects or variants of objects, and may not be repeatedly labeled and/or described. Dimensions of components and features shown in the figures are chosen for convenience or clarity of presentation. For convenience or clarity, some elements or structures are not shown or shown only partially and/or with different perspective or from different point of views.

FIG. 1 illustrates an embodiment of a medicament device disclosed herein in use;

FIG. 2 is a partially exploded view of the medicament device seen in FIG. 1 with sheath cap attached at the bottom end of the device;

FIG. 3A is a perspective view of the medicament device seen in FIG. 2;

FIG. 3B is a fully exploded view of the medicament device seen in FIG. 2;

FIG. 4A is a front view of the medicament device seen in FIG. 2;

FIG. 4B is a sectional view of the medicament device taken along line 4B-4B seen in FIG. 4A;

FIG. 5A is a front view of the medicament device seen in FIG. 2 with the sheath cap removed;

FIG. 5B is a sectional view of the medicament device taken along line 5B-5B seen in FIG. 5A;

FIG. 6A is a front view of the medicament device seen in FIG. 1 disposed above the site to be injected;

FIG. 6B is a sectional view of the medicament device and site taken along line 6B-6B seen in FIG. 6A;

FIG. 7A is a front view of the medicament device seen in FIG. 1, wherein the sheath is touching the skin of the site to be injected;

FIG. 7B is a sectional view of the medicament device and site taken along line 7B-7B seen in FIG. 7A;

FIG. 8A is a front view of the medicament device seen in FIG. 1, wherein the needle of the syringe has been inserted into the skin;

FIG. 8B is a sectional view of the medicament device and site taken along line 8B-8B seen in FIG. 8A;

FIG. 9A is a front view of the medicament device seen in FIG. 1, wherein medicament contained in the syringe is injected into the site;

FIG. 9B is a sectional view of the medicament device and site taken along line 9B-9B seen in FIG. 9A;

FIG. 10A is a front view of the medicament device seen in FIG. 1, wherein the device is in a partially released state after the medicament contained in the syringe has been injected into the site;

FIG. 10B is a sectional view of the medicament device and site taken along line 10B-10B seen in FIG. 10A;

FIG. 11A is a front view of the medicament device seen in FIG. 1, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site;

FIG. 11B is a sectional view of the medicament device and site taken along line 11B-11B seen in FIG. 11A;

FIG. 12A is a front view of the medicament device seen in FIG. 1 disposed directly above the site after injection;

FIG. 12B is a sectional view of the medicament device and site taken along line 12B-12B seen in FIG. 12A;

FIG. 13 illustrates a partially exploded view of another embodiment of a medicament device disclosed herein;

FIG. 14A is a perspective view of the medicament device seen in FIG. 13;

FIG. 14B is a fully exploded view of the medicament device seen in FIG. 13;

FIG. 15A is a front view of the medicament device seen in FIG. 13;

FIG. 15B is a side view of the medicament device seen in FIG. 13;

FIG. 15C is a sectional view of the medicament device taken along line 15C-15C seen in FIG. 15A;

FIG. 15D is a sectional view of the medicament device taken along line 15D-15D seen in FIG. 15B;

FIG. 16A is a front view of the medicament device seen in FIG. 13 with the sheath cap removed;

FIG. 16B is a side view of the medicament device seen in FIG. 13 with the sheath cap removed;

FIG. 16C is a sectional view of the medicament device taken along line 16C-16C seen in FIG. 16A;

FIG. 16D is a sectional view of the medicament device taken along line 16D-16D seen in FIG. 16B;

FIG. 17A is a front view of the medicament device seen in FIG. 16A with the needle deployed;

FIG. 17B is a side view of the medicament device seen in FIG. 16A with the needle deployed;

FIG. 17C is a sectional view of the medicament device taken along line 17C-17C seen in FIG. 17A;

FIG. 17D is a sectional view of the medicament device taken along line 17D-17D seen in FIG. 17B;

FIG. 18A is a front view of the medicament device seen in FIG. 16A with medicament in the process of being injected;

FIG. 18B is a side view of the medicament device seen in FIG. 16A with medicament in the process of being injected;

FIG. 18C is a sectional view of the medicament device taken along line 18C-18C seen in FIG. 18A;

FIG. 18D is a sectional view of the medicament device taken along line 18D-18D seen in FIG. 18B;

FIG. 19A is a front view of the medicament device seen in FIG. 16A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site;

FIG. 19B is a side view of the medicament device seen in FIG. 16A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site;

FIG. 19C is a sectional view of the medicament device taken along line 19C-19C seen in FIG. 19A;

FIG. 19D is a sectional view of the medicament device taken along line 19D-19D seen in FIG. 19B;

FIG. 20A is a front view of the medicament device seen in FIG. 16A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site and after the device has been recapped for disposal;

FIG. 20B is a side view of the medicament device seen in FIG. 16A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site and after the device has been recapped for disposal;

FIG. 20C is a sectional view of the medicament device taken along line 20C-20C seen in FIG. 20A;

FIG. 20D is a sectional view of the medicament device taken along line 20D-20D seen in FIG. 20B;

FIG. 21A is a perspective view of the sleeve of the medicament device of FIG. 13;

FIG. 21B is a perspective view of the sheath of the medicament device of FIG. 13;

FIG. 21C is a front view of the sheath seen in FIG. 21B;

FIG. 21D is a sectional view of the sheath taken along line 21D-21D seen in FIG. 21C;

FIG. 22 illustrates a partially exploded view of yet another embodiment of a medicament device disclosed herein;

FIG. 23A is a perspective view of the medicament device seen in FIG. 22;

FIG. 23B is a fully exploded view of the medicament device seen in FIG. 22;

FIG. 24A is a front view of the medicament device seen in FIG. 22;

FIG. 24B is a side view of the medicament device seen in FIG. 22;

FIG. 24C is a sectional view of the medicament device taken along line 24C-24C seen in FIG. 24B;

FIG. 25A is a front view of the medicament device seen in FIG. 22 with the sheath cap removed;

FIG. 25B is a side view of the medicament device seen in FIG. 22 with the sheath cap removed;

FIG. 25C is a sectional view of the medicament device taken along line 25C-25C seen in FIG. 25B;

FIG. 26A is a front view of the medicament device seen in FIG. 25A with the needle deployed;

FIG. 26B is a side view of the medicament device seen in FIG. 25A with the needle deployed;

FIG. 26C is a sectional view of the medicament device taken along line 26C-26C seen in FIG. 26B;

FIG. 27A is a front view of the medicament device seen in FIG. 25A with medicament in the process of being injected;

FIG. 27B is a side view of the medicament device seen in FIG. 27A with medicament in the process of being injected;

FIG. 27C is a sectional view of the medicament device taken along line 27C-27C seen in FIG. 27B;

FIG. 28A is a front view of the medicament device seen in FIG. 25A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site;

FIG. 28B is a side view of the medicament device seen in FIG. 25A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site;

FIG. 28C is a sectional view of the medicament device taken along line 28C-28C seen in FIG. 28B;

FIG. 29A is a front view of the medicament device seen in FIG. 25A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site and after the device has been recapped for disposal;

FIG. 29B is a side view of the medicament device seen in FIG. 25A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site and after the device has been recapped for disposal;

FIG. 29C is a sectional view of the medicament device taken along line 29C-29C seen in FIG. 29B;

FIG. 30A is a perspective view of the sleeve of the medicament device of FIG. 22;

FIG. 30B is a perspective view of the sheath of the medicament device of FIG. 22;

FIG. 30C is a top view of the sheath seen in FIG. 30B;

FIG. 30D is a sectional view of the medicament device taken along line 30D-30D seen in FIG. 30C;

FIG. 30E is a perspective view of the pusher of the medicament device of FIG. 22;

FIG. 31 illustrates a partially exploded view of yet another embodiment of a medicament device disclosed herein;

FIG. 32A is a perspective view of the medicament device seen in FIG. 31;

FIG. 32B is a fully exploded view of the medicament device seen in FIG. 31;

FIG. 33A is a front view of the medicament device seen in FIG. 31;

FIG. 33B is a side view of the medicament device seen in FIG. 31;

FIG. 33C is a sectional view of the medicament device taken along line 33C-33C seen in FIG. 33B;

FIG. 34A is a front view of the medicament device seen in FIG. 32 with the sheath cap removed;

FIG. 34B is a side view of the medicament device seen in FIG. 32 with the sheath cap removed;

FIG. 34C is a sectional view of the medicament device taken along line 34C-34C seen in FIG. 34B;

FIG. 35A is a front view of the medicament device seen in FIG. 33A with the needle deployed;

FIG. 35B is a side view of the medicament device seen in FIG. 33A with the needle deployed;

FIG. 35C is a sectional view of the medicament device taken along line 35C-35C seen in FIG. 35B;

FIG. 36A is a front view of the medicament device seen in FIG. 34A with medicament in the process of being injected;

FIG. 36B is a side view of the medicament device seen in FIG. 34A with medicament in the process of being injected;

FIG. 36C is a sectional view of the medicament device taken along line 36C-38C seen in FIG. 36B;

FIG. 37A is a front view of the medicament device seen in FIG. 36A, wherein medicament contained in the syringe has been injected into the site;

FIG. 37B is a side view of the medicament device seen in FIG. 36A, wherein medicament contained in the syringe has been injected into the site;

FIG. 37C is a sectional view of the medicament device taken along line 37C-37C seen in FIG. 37B;

FIG. 38A is a front view of the medicament device seen in FIG. 37A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site;

FIG. 38B is a side view of the medicament device seen in FIG. 37A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site;

FIG. 38C is a sectional view of the medicament device taken along line 38C-38C seen in FIG. 38B;

FIG. 39A is a front view of the medicament device seen in FIG. 38A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site and after the device has been recapped for disposal;

FIG. 39B is a side view of the medicament device seen in FIG. 38A, wherein the device is in a fully released state after the medicament contained in the syringe has been injected into the site and after the device has been recapped for disposal;

FIG. 39C is a sectional view of the medicament device taken along line 39C-39C seen in FIG. 39B;

FIG. 40A is a perspective view of the sleeve of the medicament device of FIG. 31;

FIG. 40B is a perspective view of the sheath of the medicament device of FIG. 31;

FIG. 40C is a side view of the sheath of the medicament device of FIG. 31;

FIG. 40D is a sectional view of the top taken along line 40D-40D seen in FIG. 40C;

FIG. 41A is a perspective view of the pusher of the medicament device of FIG. 31;

FIG. 41B is a side view of the top of the device of FIG. 31; and

FIG. 41C is a perspective view of the top taken along line 41C-41C seen in FIG. 41B.

DETAILED DESCRIPTION

For safety and accuracy, injection by syringe requires skilled technique with formal training. Steps include uncapping the needle, piercing the membrane and drawing medicament from a vial, aligning the plunger tip with respective indices to measure a required dose, correctly inserting the needle into a proper injection site, squeezing the syringe plunger while keeping the syringe stable, and recapping the bio-hazardous needle. Issues with injection by syringe include aspiring incorrect dosage, lack of safe portability, tricky syringe manipulation in administering shot, accidental needle sticks, and unsuitable syringe disposal.

Related devices that automate injection include what is commonly referred to as an auto-injector. A conventional auto-injector contains a custom, spring-loaded and pre-filled syringe, which, when triggered by pressured contact, releases a spring-loaded needle into the injection site, squirting in the dose of medicament. Issues with auto-injectors include confusing labeling, unlocking of any safety mechanism, determining where on the device the needle will exit, and accidentally firing the device into a finger by touching the actuator tip.

Accordingly, a medicament device solving these and other problems is desired.

FIGS. 1-12B illustrate an embodiment of a device 100 for administering medicament using a conventional pre-filled syringe 150 such as 1 ml Becton Dickinson tuberculin syringe filled with epinephrine. Syringe 150 may comprise barrel 152, plunger 156 that slides within barrel 152, and needle 158. The barrel 152 typically has flanges 154 at one end that aid in pushing the plunger 156 through the barrel 152 containing medicament (not shown). Depending on the intended use of device 100, the medicament may be injected into a site 180 such as a deltoid, triceps, quadriceps or the like of a user or patient.

Medicament device 100 preferably comprises a body assembly 102, a sheath cap 106 at one end of the assembly 102, and a plunger spring 130 and housing cap 104 at the other end of the assembly 102.

Body assembly 102 may be comprised of a housing 108 containing sheath 110, locking mechanism 112, sheath clip 118, and sheath spring 114. The locking mechanism 112 preferably comprises a sheath lock 116. The sheath clip 118 disposed in an annular groove within housing 108. The sheath clip 118 retains the needle sheath 110 during handling of the device 100 until needle 158 insertion.

As best seen in FIG. 3B, housing 108 is generally tubular in shape with a top and an opposing bottom. The housing 108 may have a generally wider opening at the top compared to the bottom to be able to receive a conventional syringe 150 placed into the housing 108 from the top. The overall length of the housing 108 is about the same length of barrel 152 of syringe 150 158. Similarly, the overall length of sheath 110 is also about the same length of barrel 152 of syringe 150.

The top of housing 108 is also configured to receive the sheath lock 116. The sheath lock 116 itself has an opening at one end with a slot therein configured to receive and frictionally engage the flanges 154 of syringe 150.

The bottom of the housing 108 is configured to receive the sheath 110 wherein the sheath 110 may freely slide within the housing 108. Sheath lock 116 is not permitted to slide within housing 108 but instead is held firmly in place within housing 108.

When assembled, the entire syringe 150 with its needle 158 is encased within the device 100. Sheath cap 106 and sheath 110 surround the needle 158 when the device 100 is not in use. Housing cap 104 seals the top of the housing 108, wherein one end of plunger spring 130 abuts cap 104 while the other end of spring 130 abuts the flanges 154 of the syringe 150.

FIGS. 4A-12B show the medicament device 100 in various stages of use. FIGS. 4A and 4B respectively show a front and sectional view of the device 100 fully assembled and capped by cap 106 for safe storage and transportation. FIGS. 5A and 5B respectively show a front and sectional view of the device 100 with cap 106 removed. FIGS. 6A and 6B respectively show a front and sectional view of the device 100 with cap 106 removed, wherein the sheath 110 is disposed directly above a site 180 to be injected once the needle 158 passes through skin 182. FIGS. 7A and 7B respectively show a front and sectional view of the device 100 with cap 106 removed, wherein sheath 110 is touching site 180 to be injected. FIGS. 8A and 8B respectively show a front and sectional view of the device 100 with cap 106 removed, wherein the needle 158 is deployed and passing through skin 182 and sheath spring 114 can be seen compressed. FIGS. 9A and 9B respectively show a front and sectional view of the device 100 with cap 106 removed to deliver medicament to the site 180 and produce an audible clip from the sheath lock 112 snapping past the end of the needle sheath 110. Both sheath spring 114 and plunger spring 130 can be seen compressed in FIG. 9.

FIGS. 10A and 10B respectively show a front view and sectional view of the device 100 with cap removed, wherein the device 100 is in a partially released state after the medicament contained in the syringe 150 has been injected into the site 180. FIGS. 11A and 11B respectively show a front view and sectional view of the device 100 with cap removed, wherein the device 100 is in a fully released state after the medicament contained in the syringe 150 has been injected into the site 180. FIGS. 12A and 12B respectively show a front view and sectional view of the device 100 with cap removed, wherein the device 100 is disposed above the site 180 after injection.

In typical operation, the cap assembly 106 is removed and the sheath 110 is placed against an intended injection site 180. The user then pushes down on the device 100. Continued pushing causes spring-loaded sheath 110 to retract into the housing 108, progressively exposing the syringe needle 158 until completely inserted into the injection site 180. As the stroke is continued beyond the full insertion of the needle 158, the proximal edge of the spring-loaded sheath 110 contacts the underside of the flanges 154 of the syringe barrel 152. Because the movement of the barrel 152 is constrained by the housing 108, the plunger 156 moves within its stationary barrel 152, expelling medicament through the needle 158. The sheath spring 114 requires less compression force than the syringe plunger spring 130, the effect being that the primary stroke lets the needle 158 pierce the skin 182 while the needle sheath 110 retracts. The secondary and culminating stroke actuates the plunger 156, effectively dispensing the bolus of medicament only when the needle 158 is fully inserted into the skin 182. In addition to feeling the device 100 bottom out, the user feels and hears a click confirming stroke completion. The shot having been administered, the user stops pushing down on the device 100 whereby the needle 158 is withdrawn as the spring-loaded sheath 110 extends and locks with a second click upon full extension preventing further use of the device 110. Thus, the sheath lock 116 retains the needle sheath 110 in an extended position that covers the needle 158 of the syringe 150 after injection is complete.

FIGS. 13-21 illustrate another embodiment of a device 200 for administering a medicament such as by an injection using a conventional pre-filled syringe 250. Such a syringe 250 may comprise a barrel 252, plunger 256 that slides within barrel 252, and needle 258. The barrel 252 typically has flanges 254 at one end that aid in pushing the plunger 256 through the barrel 252 containing medicament (not shown) to be administered by a user or patient.

Medicament device 200 preferably comprises a body assembly 202, a sheath cap 206 at end of the assembly 202, and a housing cap 204 with its optional label 224 at the other end of the assembly 202.

Body assembly 202 may be comprised of a housing 208 containing sheath 210 with its optional sheath seal 226, locking mechanism 212, and sheath spring 214. The locking assembly 212 preferably comprises a sleeve 216 having sleeve tracks 218 configured to receive one or more sheath pins 220 protruding from the interior of sheath 210, as well as sheath snaps 222 disposed about the interior of sheath 210 and protruding therefrom, as illustrated in FIGS. 21A-21D. Sheath seal 226 may serve to seal the chamber of syringe 250 until pierced by the needle 258.

As best seen in FIG. 14B, housing 208 is generally tubular in shape with a top and an opposing bottom. The top of housing 208 is configured to receive and frictionally engage a conventional syringe 250 placed into the housing 208 from the top. The top of housing 208 is also configured to receive the sleeve 216 having an opening at one end configured to receive syringe 250. The bottom of the housing 208 is configured to receive the sheath 210 wherein the sheath 210 may freely slide within the housing 208.

The overall length of the housing 208 is about the same length of the barrel 252 of conventional syringe 250. Similarly, the overall length of sheath 210 with its sheath fingers 228 is also about the same length of the barrel 252.

When assembled, the entire syringe 250 with its needle 258 is encased within the device 200. Sheath cap 206 and sheath 210 surround the needle 258 when the device 200 is not in use. Housing cap 204 seals the top of the housing 208.

FIGS. 15A-20D show the medicament device 200 in various stages of use. FIGS. 15A-15D show the device 200 fully assembled and capped by cap 206 for safe storage and transportation. FIGS. 16A-16D show the device 200 with cap 206 removed. FIGS. 17A-17D show the device 200 in a stage whereby the needle 258 is deployed to deliver medicament. FIGS. 18A-18D show the device 200 with spring 214 in a compressed state wherein medicament has been delivered or is being delivered. FIGS. 19A-19D show the device 200 in a fully released state after the medicament has been delivered. FIGS. 20A-20D show the device 200 in a fully released and locked state with the device being recapped for disposal.

In typical operation, the cap assembly 206 is removed and the sheath 210 is then placed against an intended injection site. The user then pushes down on the device 200. Continued pushing causes spring-loaded sheath 210 to retract into the housing 208, progressively exposing the syringe needle 258 until it is completely inserted into the injection site, fully compressing sheath 210 wherein sheath fingers 228 slide within housing body 208. Concurrently, sheath pins 220 found on the internal surface of sliding sheath 210 track in sleeve tracks 218, effectively guiding and rotating the sleeve 216 concentrically as the sheath 210 draws in and into bifurcated sleeve tracks 218.

When sheath 210 is fully compressed into body 208, sheath fingers 228 contact and spread snaps 222 to permit the plunger 256 to slide within barrel 252 and thereby expel medicament through syringe needle 258.

The shot having been administered, the device 200 is then removed from the injection site, withdrawing syringe needle 258 and allowing spring-loaded sheath 210 to re-extend from the body 208 due to the biasing force of sheath spring 214. Sheath pins 220 track in the straight and slightly longer bifurcation found in the now-rotated sleeve tracks 218. At full extension, sheath 210 bottoms out at a position slightly more extended than its initial position, thus allowing sheath snaps 222 to engage and lock out sheath 210 for the purpose of protecting syringe needle 258, thereby preventing further use of the device 200.

The disclosed inventions advantageously may use a conventional syringe pre-loaded by the user for pre-filled, portable injections (e.g., insulin, epinephrine). The device 100, 200 may be produced in varying lengths and sizes to accommodate different syringe sizes (e.g., 0.3 mL, 1 mL, 3 mL). The device 100, 200 may also be produced in a length that precludes over-filling the syringe beyond a set dosage, and thus avoid a potential overdose.

The disclosed inventions may also function with any prescribed quantity of medicament equal to or less than full capacity. For example, the device 100, 200 may be adjusted to dispense varying doses of medicament by means of a coarsely threaded cap, which may be adjusted to vary the travel length of syringe plunger, with indices showing the relative amount of medicament to be dispensed.

The housing of the device 100, 200 may also include a window to provide a direct view of the medication. Such a window may be circumscribed with a color that, when matched with the medicament color as viewed through said window, indicates the medicament has expired. In such a situation, the syringe may advantageously be changed out for a new syringe with non-expired medicament.

The sheath may be marked with color or graphics to let the user know the syringe needle is fully inserted (triggering medicament injection). In the alternative, a battery-powered light emitting diode or the like may illuminate to indicate the syringe needle is fully inserted.

The housing may be made of a transparent material that reveals the inner functioning of the device, including revealing the amount of medicament in syringe. The housing may also incorporate instructional graphics.

The device 100, 200 may include a peel-off-cover antiseptic pad for the purpose of cleaning the injection site. Such a pad may be adhered to the housing cap, for example.

The housing cap may permanently lock when inserted into housing, sealing in the syringe to assure single-use only. In the alternative, the housing cap may be removable to change out the syringe as desired so the device may be further used. If desired to limit reuse of device 100, 200, then the housing cap may be removable by means of a special tool.

The device 100, 200 may be made of disposable, single-use materials, or alternatively, made of reusable materials that could withstand repeated sterilization. Regardless of the materials used, the device 100, 200 may incorporate a peel tab or breakaway part that renders the device non-functional after a single use, insuring single-use only.

The medical device 100, 200 may also include a split thrust washer located between the syringe flanges and the housing cap that deforms when squeezed to provide a tactile and audible click when the plunger is fully depressed, letting the user know that the stroke is complete, all medicament is dispensed, and the shot has been successfully administered.

The device 100, 200 may integrate a voice-chip to provide audible instructions and status such as when a medicament has expired or is nearing the expiration date. Similarly, the device 100, 200 may integrate a chemical or mechanical timer to indicate when a determined number of days have passed since syringe filling, indicating expiration of contents. Such a timer may be activated when the housing cap is closed to begin the countdown to medicament expiration.

The device 100, 200 may include a shrink-wrap thermoplastic with graphics wherein the wrap is applied to seal and retain the protective cap and then peeled away for use. Similarly, the housing body may be sheathed in shrink-wrap thermoplastic with graphics showing instructional information, expiration date, custom branding, or the like.

The device 100, 200 may include a flat surface on an otherwise cylindrical body to keep the device from rolling. Such a flat surface may be used to print indicia via a felt-tip marker or the like.

The device 100, 200 may include a rotating collar on an otherwise cylindrical body that is positioned by the assembler or user to show the loaded medicament dose. The rotating collar may then be locked into place by virtue of device assembly.

The device 100, 200 may include a metal sleeve within housing, which when pre-chilled with ice or refrigeration, provides cooling for heat-sensitive medicament. In the alternative or in addition thereto, the device 100, 200 may be shaped to fit into a refrigerated chiller to pre-cool heat-sensitive medicament during transportation.

The housing may be configured to contain a plurality of syringes in the event that administration of initial injection is inadequate to treat the present condition (e.g., epinephrine administration for anaphylaxis typically calls for a second dose if symptoms do not abate in a timely manner) or for convenience of having more than one injection at hand (e.g., fertility injections are typically timed hourly).

The device 100, 200 may also be used for oral medication dispensation, concealing a standard syringe and its association with needles.

It should now be apparent that the disclosed inventions have many advantages over conventional devices. Conventional auto-injectors, upon trigger-release, automatically inject needle and medicament, presumably into an intended injected site. Unlike auto-injectors, the disclosed inventions do not automatically insert the needle, an advantage in avoiding accidental actuation that happens with conventional auto-injectors.

Moreover, devices 100, 200 rely on manual action to insert the needle at the injection site, like a standard syringe, making needle sticks less likely than when using and auto-injector, which fires its needle upon contact with any surface, including hands, thumbs, and fingers. The disclosed inventions 100, 200 also inject medicament only after the needle is fully inserted, unlike conventional auto-injectors, which inject medicament immediately upon trigger release. Safety issues, such as a child accidentally firing an adult-dosage auto-injector and thereby receiving twice the recommended amount of medicament for their size, are thus avoided. Also avoided is the dispensing of medicament along the needle tract during insertion, where medicament may not get to its intended target area as may occur with conventional auto-injectors.

The disclosed inventions 100, 200 also facilitate hypodermic injection using an evolved, standard ubiquitous syringe rather than a proprietary or custom syringe that may fail. Moreover, the disclosed inventions 100, 200 may be filled to a prescribed dose of medicament rather than “one-dose-fits-all” as found with auto-injectors and factory-filled syringes. Such pre-loading of medicament may conveniently be done in a domestic setting such as the user's home, in a clinical setting such as a doctor's office, or in an institutional setting such as a school. Indeed, as the contained syringe is pre-filled to a prescribed dosage, the disclosed inventions 100, 200 are ready for use and may be rapidly deployed and used in emergency or military situations.

The sheath cap of the disclosed inventions also acts as both protector and safety cover against accidental activation. Moreover, after use, the locking mechanism of the device 100, 200 protects the needle from being extended from the sheath when the sheath cap is not present, resulting in another advantageous and novel safety feature.

The disclosed inventions 100, 200 are also simpler and safer than administering shots with a standard syringe aspirating from a standard vial. Fortunately, the use of the disclosed inventions is not dissimilar to the customary administering of a typical shot. Such action is in contrast to the violent firing of a needle into skin as is done with a conventional auto-injector. Moreover, because the contained syringe is pre-filled to a prescribed dosage, an unskilled user may quickly and safely administer a shot.

Finally, the disclosed injectors 100, 200 have only two actions to administer a shot: removing the housing cap and pushing down the device on an intended injection site. Conventional auto-injectors require removal from a carrier tube, removal of a locking key, and then pushing onto the intended injection site.

FIGS. 22-30 illustrate another embodiment of a device 300 for administering a shot from a standard pre-filled syringe 316. Such a syringe 316 may comprise a barrel 320, plunger 318 that slides within barrel 320, and needle 324. The barrel 320 typically has flanges 321 at one end that aid in pushing the plunger 318 through the barrel 320 containing medicament (not shown) to be administered by a user or patient.

Medicament device 300 preferably comprises a body assembly 302, a cap assembly 304 at one end of the body assembly 302, and a top assembly 306 at the other end of the body assembly 302 with its optional label 308.

Body assembly 302 may be comprised of a body 330 containing sheath 334 with its optional sheath seal 336, locking assembly 326, and sheath spring 332. The locking assembly 326 preferably comprises a sleeve 328 having a sleeve ledge 344 and sleeve tracks 342 configured to receive one or more sheath pins 348 protruding from the interior of sheath 334, as well as sheath snaps 350 disposed about the interior of sheath 334 and protruding therefrom, as illustrated in FIGS. 30A-30D. Sheath seal 336 may serve to seal the chamber of syringe 316 until pierced by the needle 324.

Cap assembly 304 may include cap 338. Top assembly 306 may include top 310, pusher spring 312, pusher 314, and top label 308. Sheath spring 332 requires less compression force than the pusher spring 312.

As best seen in FIG. 22, body 330 is generally tubular in shape with a top and an opposing bottom. The top of body 330 is configured to receive and frictionally engage conventional syringe 316 placed into body 330 from the top. The top of body 330 is also configured to receive the sleeve 328 having an opening at one end configured to receive syringe 316. The bottom of the body 330 is configured to receive the sheath 334 wherein the sheath 334 may freely slide within body 330.

The overall length of body 330 is about the same length of the barrel 320 of conventional syringe 316. Similarly, the overall length of sheath 334 with its sheath fingers 340 is also about the same length of the barrel 320.

When assembled, the entire syringe 316 with its needle 324 is encased within the device 300. Sheath cap 338 and sheath 334 surround the needle 316 when the device 300 is not in use. Cap 338 then seals body 330.

FIGS. 24A-29C show the medicament device 300 in various stages of use. FIGS. 24A-24C show the device 300 fully assembled and capped by cap 338 for safe storage and transportation. FIGS. 25A-25C show the device 300 with cap 338 removed. FIGS. 26A-26C show the device 300 in a stage whereby the needle 324 is deployed to deliver medicament. FIGS. 27A-27C show the device 300 with spring 332 in a compressed state wherein medicament has been delivered or is being delivered. FIGS. 28A-28C show the device 300 in a fully released state after the medicament has been delivered. FIGS. 29A-29C show the device 300 in a fully released and locked state with the device 300 being recapped for disposal.

In typical operation, there are three stages of use: start, insert, and plunge, wherein sheath fingers 346 push snaps 350 releasing pusher 314 that depresses syringe plunger 318 dispensing syringe 316 contents. The user begins by removing the cap assembly 304. The sheath 334 is then placed against an intended injection site (e.g., deltoid, triceps, quadriceps), with the user then pushing down on the device 300. Continued pushing causes spring-loaded sheath 334 to retract into the body 330, progressively exposing the syringe needle 324 until it is completely inserted into the injection site, fully compressing sheath 334 wherein sheath fingers 346 slide within body 330. Concurrently, sheath pins 348 found on the internal surface of sliding sheath 334 track in sleeve tracks 342, effectively guiding and rotating the sliding sleeve 328 concentrically as the sheath 334 draws in, guided by bifurcated sleeve tracks 334, as best seen in FIG. 30A.

When sheath 334 is fully compressed into body 330, sheath fingers 340 contact and spread snaps 350, releasing pusher 314 to slide within the body 330 as driven by the compressed pusher spring 312. Pusher 314 then depresses syringe plunger 318 fully into the syringe barrel 320, expelling the medicament through syringe needle 324.

The shot having been administered, the device 300 is then removed from the injection site, withdrawing syringe needle 324 and allowing spring-loaded sheath 334 to re-extend from the body 330 due to the biasing force of sheath spring 332. Sheath pins 348 track in the straight and slightly longer bifurcation found in the now-rotated sleeve tracks 342. At full extension, sheath 334 bottoms out at a position slightly more extended than its initial position, thus allowing sheath snaps 350 to engage and lock out sheath 334 for the purpose of protecting syringe needle 324, thereby preventing further use of the device 300.

The syringe 316 of the device 300 may be pre-loaded by the user for pre-filled, portable injections (e.g., insulin, epinephrine). The device 300 may be produced in varying lengths and sizes to accommodate different syringe sizes (e.g., 0.3 mL, 1 mL, 3 mL). The device 300 may also be adjusted to dispense varying doses of medicament by means of a coarsely threaded cap assembly 304, which may be adjusted to vary the travel length of syringe plunger 318, with indices showing the relative amount of medicament to be dispensed. The body 330 may also include a window to provide a direct view of the medication. Such a window may be circumscribed with a color that, when matched with the medicament color as viewed through said window, indicates the medicament has expired. In such a situation, the syringe 316 may advantageously be changed out for a new syringe with non-expired medicament.

The sheath 334 may be marked with color or graphics to let the user know the syringe needle 324 is fully inserted (triggering medicament injection). In the alternative, a battery-powered light emitting diode or the like may illuminate to indicate the syringe needle 324 is fully inserted. The sleeve 328 may also be marked with color or graphics visible through a window in the body 330 to let the user know injection is complete.

The body 330 may be made of a transparent material that reveals the inner functioning of the device 300, including revealing the amount of medicament in syringe 316. The body 330 may alternatively be made of transparent or translucent material and wrapped with an opaque label in a manner that reveals the medicament level in syringe 316 through a label window. The body 330 may similarly incorporate instructional graphics.

The device 300 may include a peel-off-cover antiseptic pad for the purpose of cleaning the injection site. Such a pad may be adhered to the top or cap assemblies, 306, 304, for example.

The top assembly 306 may permanently lock when inserted into body 330, sealing in syringe 316 to assure single-use only. In the alternative, the top assembly 306 may be removable to change out syringe 316 as desired so the device 300 may be further used. If desired to limit device 300 reuse, the top assembly 306 may be removable by means of a special tool.

The cap 338 may be press-fit onto body 330 for removal by twisting off. Cap 338 may be press-fit onto body 330 with a cam feature to facilitate removal as it is twisted. The cap 338 may also include an attachment point for a lanyard. The cap 338 may also be integrated with a label that covers the whole device 300, with scoring marks to tear off the portion of the label that is acting as a cap. Similarly, the amount and/or type of medicament may be printed graphically on the proximal body tip.

Sheath 346 may lock upon extension after the needle 324 is withdrawn and then unlocked by a tool such as a pick, paper clip, or small screwdriver.

The device 300 may be made of disposable, single-use materials, or alternatively, made of reusable materials that could withstand repeated sterilization. Regardless of the materials used, device 300 may incorporate a peel tab or breakaway part that renders the device 300 non-functional after a single use, insuring single-use only.

The device 300 may also include a split thrust washer located between the syringe flanges 321 and the body cap 338 that deforms when squeezed to provide a tactile and audible click when the plunger 318 is fully-depressed, letting the user know that the stroke is complete, all medicament is dispensed, and the shot has been successfully administered.

The device 300 may integrate a voice-chip to provide audible instructions and status such as when a medicament has expired or is nearing the expiration date. Similarly, the device 300 may integrate a chemical or mechanical timer to indicate when a determined number of days have passed since syringe filling, indicating expiration of contents. Such a timer may be activated when top assembly 306 is closed to begin the countdown to medicament expiration.

The device 300 may include a shrink-wrap thermoplastic with graphics wherein the wrap is applied to seal and retain the protective cap 338 and then peeled away for use. Similarly, the body 330 may be sheathed in shrink-wrap thermoplastic with graphics showing instructional information, expiration date, custom branding, or the like.

The device 300 may include a flat surface on an otherwise cylindrical body 330 to keep the device 300 from rolling. Such a flat surface may be used to print indicia via a felt-tip marker or the like.

The device 300 may include a rotating collar on an otherwise cylindrical body 330 that is positioned by the assembler or user to show the loaded medicament dose. The rotating collar may then be locked into place by virtue of device assembly.

The device 300 may include a metal sleeve 328 within body 330, which when pre-chilled with ice or refrigeration, provides cooling for heat-sensitive medicament. In the alternative or in addition thereto, the device 300 may be shaped to fit into a refrigerated chiller to pre-cool heat-sensitive medicament during transportation.

The body 330 may be configured to contain a plurality of syringes in the event that administration of initial injection is inadequate to treat the present condition (e.g., epinephrine administration for anaphylaxis typically calls for a second dose if symptoms do not abate in a timely manner) or for convenience of having more than one injection at hand (e.g., fertility injections are typically timed hourly).

The device 300 may also be used for oral medication dispensation, concealing a standard syringe and its association with needles.

The device 300 may incorporate a microchip, such as a radio-frequency identification or near-field communication chip, for geolocation, product information, expiration information, or other such status of the device 300 and its contents.

FIGS. 31-41 illustrate another embodiment of a device 400 for administering a shot from a standard pre-filled syringe 416. Such a syringe 416 may comprise a barrel 420, plunger 418 that slides within barrel 420, and needle 424. The barrel 420 typically has flanges 421 at one end that aid in pushing the plunger 418 through the barrel 420 containing medicament (not shown) to be administered by a user or patient.

Medicament device 400 preferably comprises a body assembly 402, a cap assembly 404 at one end of the body assembly 402, and a top assembly 406 at the other end of the body assembly 402 with its optional label 408.

Body assembly 402 may be comprised of a sheath 432 with its optional sheath seal 434, locking mechanism 426, and sheath spring 430. The locking assembly 426 preferably comprises a sleeve 428 having a sleeve ledge 448, sheath catch 452, and sleeve tracks 446 configured to receive one or more sheath pins 454 protruding from the interior of sheath 432, as well as sheath snaps 456 disposed about the interior of sheath 432 and protruding therefrom, as illustrated in FIGS. 40A-40D. Sheath seal 434 may serve to seal the chamber of syringe 416 until pierced by the needle 424.

Cap assembly 404 may include cap 436. Top assembly 406 may include top 410, pusher spring 412, pusher 414 having pusher stops 438, pusher first snaps 440, pusher second snaps 442, and top label 408. Sheath spring 430 requires less compression force than the pusher spring 412.

As best seen in FIG. 31, top 410 is generally tubular in shape with a top and an opposing bottom. The top of top 410 is configured to receive and frictionally engage conventional syringe 416 placed into top 410 from the top. The top of top 410 is also configured to receive the sleeve 428 having an opening at one end configured to receive syringe 416. The bottom of top 410 is configured to receive the sheath 432 wherein the sheath 432 may freely slide within top 410.

The overall length of top 410 is about the same length of the barrel 420 of conventional syringe 416. Similarly, the overall length of sheath 432 with its sheath fingers 450 is also about the same length of the barrel 420.

When assembled, the entire syringe 416 with its needle 424 is encased within the device 400. Sheath cap 436 and sheath 432 surround the needle 416 when the device 400 is not in use. Cap 436 then seals top 410.

FIGS. 33A-39C show the medicament device 400 in various stages of use. FIGS. 33A-33C show the device 400 fully assembled and capped by cap 436 for safe storage and transportation. FIGS. 34A-34C show the device 400 with cap 436 removed. FIGS. 35A-35C show the device 400 in a stage whereby the needle 424 is deployed to deliver medicament. FIGS. 36A-36C show the device 400 with spring 430 in a compressed state. FIGS. 37A-37C show the device 400 with spring 412 in an uncompressed state wherein medicament has been delivered or is being delivered. FIGS. 38A-38C show the device 400 in a fully released state after the medicament has been delivered. FIGS. 39A-39C show the device 400 in a fully released and locked state with the device 400 being recapped for disposal.

In typical operation, there are three stages of use: start, insert, and plunge, wherein sheath fingers 450 push snaps 456 releasing pusher 414 that depresses syringe plunger 418 dispensing syringe 416 contents. The user begins by removing the cap assembly 404. The sheath 432 is then placed against an intended injection site (e.g., deltoid, triceps, quadriceps), with the user then pushing down on the device 400. Continued pushing causes spring-loaded sheath 432 to retract into top 410, triggering the syringe needle 424 until it is completely inserted into the injection site, fully compressing sheath 432 wherein sheath fingers 450 slide within top 410. Concurrently, sheath pins 454 found on the internal surface of sliding sheath 334 track in sleeve tracks 342, effectively guiding and rotating the sliding sleeve 432 concentrically as the sheath 432 draws in, guided by bifurcated sleeve tracks 447, as best seen in FIG. 40A.

When sheath 432 is fully compressed into top 410, sheath fingers 450 contact and spread snaps 456, releasing pusher 414 to slide within top 410 as driven by the compressed pusher spring 416. Pusher 414 then depresses syringe plunger 418 fully into the syringe barrel 420, expelling the medicament through syringe needle 424.

The shot having been administered, the device 400 is then removed from the injection site, withdrawing syringe needle 424 and allowing spring-loaded sheath 432 to re-extend from top 410 due to the biasing force of sheath spring 430. Sheath pins 454 track in the straight and slightly longer bifurcation found in the now-rotated sleeve tracks 446. At full extension, sheath 432 bottoms out at a position slightly more extended than its initial position, thus allowing sheath snaps 456 to engage and lock out sheath 432 for the purpose of protecting syringe needle 424, thereby preventing further use of the device 400.

The syringe 416 of the device 400 may be pre-loaded by the user for pre-filled, portable injections (e.g., insulin, epinephrine). The device 400 may be produced in varying lengths and sizes to accommodate different syringe sizes (e.g., 0.3 mL, 1 mL, 3 mL). The device 400 may also be adjusted to dispense varying doses of medicament by means of a coarsely threaded cap assembly 404, which may be adjusted to vary the travel length of syringe plunger 418, with indices showing the relative amount of medicament to be dispensed. The top 410 may also include a window to provide a direct view of the medication. Such a window may be circumscribed with a color that, when matched with the medicament color as viewed through said window, indicates the medicament has expired. In such a situation, the syringe 416 may advantageously be changed out for a new syringe with non-expired medicament.

The sheath 432 may be marked with color or graphics to let the user know the syringe needle 424 is fully inserted (triggering medicament injection). In the alternative, a battery-powered light emitting diode or the like may illuminate to indicate the syringe needle 424 is fully inserted. The sleeve 428 may also be marked with color or graphics visible through a window in the top 410 let the user know injection is complete.

The top 410 may be made of a transparent material that reveals the inner functioning of the device 400, including revealing the amount of medicament in syringe 416. The top 410 may alternatively be made of transparent or translucent material and wrapped with an opaque label in a manner that reveals the medicament level in syringe 416 through a label window. The top 410 may similarly incorporate instructional graphics.

The device 400 may include a peel-off-cover antiseptic pad for the purpose of cleaning the injection site. Such a pad may be adhered to the top or cap assemblies, 406, 404, for example.

The top assembly 406 may permanently lock when inserted into top 410, sealing in syringe 416 to assure single-use only. In the alternative, the top assembly 406 may be removable to change out syringe 416 as desired so the device 400 may be further used. If desired to limit device 400 reuse, the top assembly 406 may be removable by means of a special tool.

The cap 436 may be press-fit onto top 410 for removal by twisting off. Cap 436 may be press-fit onto top 410 with a cam feature to facilitate removal as it is twisted. The cap 436 may also include an attachment point for a lanyard. The cap 436 may also be integrated with a label that covers the whole device 400, with scoring marks to tear off the portion of the label that is acting as a cap. Similarly, the amount and/or type of medicament may be printed graphically on the proximal body tip.

Sheath 432 may lock upon extension after the needle 424 is withdrawn and then unlocked by a tool such as a pick, paper clip, or small screwdriver.

The device 400 may be made of disposable, single-use materials, or alternatively, made of reusable materials that could withstand repeated sterilization. Regardless of the materials used, device 400 may incorporate a peel tab or breakaway part that renders the device 400 non-functional after a single use, insuring single-use only.

The device 400 may also include a split thrust washer located between the syringe flanges 421 and the body cap 436 that deforms when squeezed to provide a tactile and audible click when the plunger 418 is fully-depressed, letting the user know that the stroke is complete, all medicament is dispensed, and the shot has been successfully administered.

The device 400 may integrate a voice-chip to provide audible instructions and status such as when a medicament has expired or is nearing the expiration date. Similarly, the device 400 may integrate a chemical or mechanical timer to indicate when a determined number of days have passed since syringe filling, indicating expiration of contents. Such a timer may be activated when top assembly 406 is closed to begin the countdown to medicament expiration.

The device 400 may include a shrink-wrap thermoplastic with graphics wherein the wrap is applied to seal and retain the protective cap 436 and then peeled away for use. Similarly, the top 410 may be sheathed in shrink-wrap thermoplastic with graphics showing instructional information, expiration date, custom branding, or the like.

The device 400 may include a flat surface on an otherwise cylindrical top 410 to keep the device 400 from rolling. Such a flat surface may be used to print indicia via a felt-tip marker or the like.

The device 400 may include a rotating collar on an otherwise cylindrical top 410 that is positioned by the assembler or user to show the loaded medicament dose. The rotating collar may then be locked into place by virtue of device assembly.

The device 400 may include a metal sleeve 428 within top 410, which when pre-chilled with ice or refrigeration, provides cooling for heat-sensitive medicament. In the alternative or in addition thereto, the device 400 may be shaped to fit into a refrigerated chiller to pre-cool heat-sensitive medicament during transportation.

The top 410 may be configured to contain a plurality of syringes in the event that administration of initial injection is inadequate to treat the present condition (e.g., epinephrine administration for anaphylaxis typically calls for a second dose if symptoms do not abate in a timely manner) or for convenience of having more than one injection at hand (e.g., fertility injections are typically timed hourly).

The device 400 may also be used for oral medication dispensation, concealing a standard syringe and its association with needles.

The device 400 may incorporate a microchip, such as a radio-frequency identification or near-field communication chip, for geolocation, product information, expiration information, or other such status of the device 400 and its contents.

It should now be apparent that the disclosed inventions 300, 400 have many advantages over conventional devices such as those discussed previously. For example, the disclosed inventions 100, 200, 300, or 400 facilitate hypodermic injection using an evolved, standard ubiquitous syringe rather than a proprietary or custom syringe that may fail. Moreover, the disclosed inventions may be filled to a prescribed dose of medicament rather than “one-dose-fits-all” as found with auto-injectors and factory-filled syringes. Such pre-loading of medicament may conveniently be done in a domestic setting such as the user's home, in a clinical setting such as a doctor's office, or in an institutional setting such as a school. Indeed, as the contained syringe is pre-filled to a prescribed dosage, the disclosed inventions are ready for use and may be rapidly deployed and used in emergency or military situations.

The sheath cap of the disclosed inventions also acts as both protector and safety cover against accidental activation.

The disclosed inventions are simpler and safer than administering shots with a standard syringe aspirating from a standard vial. Fortunately, the use of the disclosed inventions is not dissimilar to the customary administering of a typical shot. Such action is in contrast to the violent firing of a needle into skin as is done with a conventional auto-injector. Moreover, because the contained syringe is pre-filled to a prescribed dosage, an unskilled user may quickly and safely administer a shot.

The disclosed inventions may also function with any prescribed quantity of medicament equal to or less than full capacity. Finally, the disclosed inventions 100, 200, 300, or 400 have only two actions to administer a shot: removing the cap, and pushing down the device on an intended injection site. Conventional auto-injectors require removal from a carrier tube, removal of a locking key, and then pushing onto the intended injection site.

While certain embodiments have been described, the embodiments have been presented by way of example only and are not intended to limit the scope of the inventions. Indeed, the medicament devices disclosed herein may be embodied in a variety of other forms. Furthermore, various omissions, substitutions, and changes in the form of the disclosed elements may be made without departing from the spirit of the inventions. 

The invention claimed is:
 1. A device for administering medicament using a conventional syringe, the device comprising: a body assembly configured to receive a conventional syringe, the body assembly having a top and an opposing bottom; and a top assembly at the top of the body assembly; wherein the body assembly comprises a sheath, a locking mechanism, and a sheath spring; wherein the locking mechanism comprises a sleeve, sleeve tracks, and one or more sheath pins, wherein the sleeve is slideably disposed at an end opposite the sheath, wherein the sheath pins protrude from the interior of the sheath, and wherein the sleeve tracks are cut within the sleeve and configured to engage the one or more sheath pins.
 2. The medicament device of claim 1, wherein the sleeve tracks are bifurcated to lock the sheath in place around a needle of a conventional syringe after use of the device to administer medicament.
 3. The medicament device of claim 1, wherein the locking mechanism further comprises sheath snaps extending from the interior of the sheath, and wherein the sheath has sheath fingers extending from one end of the sheath for engaging the sheath snaps.
 4. The medicament device of claim 1, wherein the top assembly includes a top, a pusher spring, and a pusher.
 5. The medicament device of claim 4, wherein the pusher spring requires more compression force than the sheath spring.
 6. The medicament device of claim 5, wherein the body assembly further comprises a body configured to receive the sheath, sheath spring, and a sleeve.
 7. The medicament device of claim 1, further comprising a cap assembly at the bottom of the body.
 8. The medicament device of claim 4, further comprising a cap assembly at the bottom of the top.
 9. The medicament device of claim 1, wherein the sheath is substantially the same length as a barrel of a conventional syringe. 